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Resumen de ¹h and 13c nmr spectral assignments and x-ray crystallography of n-(3-(1h-imidazol-1-yl)propyl)-2-phenylquinazolin-4-amine

Marcia Pérez-fehrmann, Victor Hugo Kesternich Martinez, Felipe Verdugo, Laurence Marcourt, Philippe Christen, Iván Brito

  • N-(3-(1H-Imidazol-1-yl)propyl)-2-phenylquinazolin-4-amine (2) was obtained by nucleophilic substitution of 1-(3-aminopropyl)-imidazole over 4-chloro-2-phenylquinazoline (1) with DMF/TEA at room temperature. The precursor and product were characterized by NMR spectroscopy. The structure of the title compound was confirmed by X-ray diffraction methods. The quinazoline fragment (2) is essentially planar and makes a dihedral angle of 66.35 ° with the imidazole plane. In the crystal packing the molecules are associated by two strong intermolecular NH----N hydrogen bonds with graph-set motif R²2(16). These pairs are linked by two π-π interactions.


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